| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6959320-6959720 | Common:4; Rare:84 | ||||
| chr12:6969947-6970428 | Common:2; Rare:260 | ||||
| chr12:6970461-6971030 | Common:28; Rare:999; Clinvar (benign):7 | ||||
| chr12:7018396-7018750 | Common:5; Rare:354 | ||||
| chr12:7018735-7019130 | Common:10; Rare:251 | ||||
| chr12:7107958-7108358 | Common:2; Rare:87 | ||||
| chr12:7108271-7108703 | Common:11; Rare:594 | ||||
| chr12:7108731-7109519 | Common:41; Rare:507 | ||||
| chr12:7127976-7128889 | Common:7; Rare:438 | ||||
| chr12:7128858-7129087 | Common:4; Rare:102 | ||||
| chr12:7129160-7129873 | Common:2; Rare:102 | ||||
| chr12:7129995-7130522 | Common:32; Rare:428 | ||||
| chr12:7131002-7131460 | Common:3; Rare:111 | ||||
| chr12:7189447-7189870 | Common:16; Rare:721; Clinvar:29; Clinvar (benign):4 | ||||
| chr12:7369250-7369630 | Rare:193 |